Canonical Allele Identifier: CA354805477

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188926A>C (hg19) ; chr3:g.142470084A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470084A>C , CM000665.2:g.142470084A>C	GRCh38
NC_000003.11:g.142188926A>C , CM000665.1:g.142188926A>C	GRCh37
NC_000003.10:g.143671616A>C	NCBI36
NG_008951.1:g.113743T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6319+2T>G MANE Select	ENSP00000343741.4:n.6319+2T>G
ENST00000513291.2:n.1503+2T>G
ENST00000654170.1:n.1162+2T>G
ENST00000656590.1:c.5109+2T>G
ENST00000661310.1:c.6127+2T>G	ENSP00000499589.1:n.6127+2T>G
ENST00000665483.1:n.174+2T>G
ENST00000666447.1:n.154+2T>G
ENST00000666943.1:n.1783+2T>G
ENST00000350721.8:c.6319+2T>G	ENSP00000343741.4:n.6319+2T>G
NM_001184.3:c.6319+2T>G	NP_001175.2:n.6319+2T>G
XM_011512924.1:c.6325+2T>G	XP_011511226.1:n.6325+2T>G
XM_011512925.1:c.6133+2T>G	XP_011511227.1:n.6133+2T>G
XR_924147.1:n.6414+2T>G
XR_924148.1:n.6414+2T>G
XR_924149.1:n.6293+2T>G
NM_001354579.1:c.6127+2T>G	NP_001341508.1:n.6127+2T>G
XR_001740179.2:n.6408+2T>G
XR_001740180.2:n.6462+2T>G
XR_001740181.2:n.6341+2T>G
XR_001740182.1:n.6293+2T>G
XR_002959543.1:n.6518+2T>G
XR_924148.2:n.6414+2T>G
NM_001184.4:c.6319+2T>G MANE Select	NP_001175.2:n.6319+2T>G
NM_001354579.2:c.6127+2T>G	NP_001341508.1:n.6127+2T>G